Canonical Allele Identifier: CA337645444
Gene: RBMY2QP HGNC NCBI

Linked Data

dbSNP Id: rs13304882

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.9981692C>G , CM000686.2:g.9981692C>G GRCh38
NC_000024.9:g.9819301C>G , CM000686.1:g.9819301C>G GRCh37
NC_000024.8:g.10429301C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651645.1:n.1003+7498G>C